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Enantioselective Synthesis of (-)-Vertinolide.
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1997
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BiosynthesisBioorganic ChemistryEngineeringBiochemistryNatural Product SynthesisNatural SciencesOrganic Chemistryβ-Tetronic AcidChiral SourceStereoselective SynthesisPharmacologySynthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringChiral Self-reproduction Method
(-)-Vertinolide, a β-tetronic acid derivative isolated from Verticillium intertextum as one of the mycotoxins, was synthesized starting from (R)-lactic acid as the chiral source by using Seebach's chiral self-reproduction method. The β-tetronic acid moiety was constructed by reductive dehydroxylation of α, β-dihydroxybutanolide with samarium(II) iodide and subsequent oxdation.